Literature DB >> 35814718

Overweight and obesity as risk factors for COVID-19-associated hospitalisations and death: systematic review and meta-analysis.

Wendemi Sawadogo1, Medhin Tsegaye1, Andinet Gizaw1, Tilahun Adera1.   

Abstract

Objective: To quantify the current weight of evidence of the association between overweight and obesity as risk factors for COVID-19-related hospitalisations (including hospital admission, intensive care unit admission, invasive mechanical ventilation) and death, and to assess the magnitude of the association and the potential dose-response relationships. Design: PubMed, Embase, Cochrane, Web of Sciences, WHO COVID-19 database and Google Scholar were used to identify articles published up to 20 July 2021. Peer-reviewed studies reporting adjusted estimates of the association between overweight or obesity and COVID-19 outcomes were included. Three authors reviewed the articles and agreed. The quality of eligible studies was assessed using the Newcastle-Ottawa Quality Assessment Scale. Random-effects meta-analysis was used to estimate the combined effects.
Results: A total of 208 studies with 3 550 997 participants from over 32 countries were included in this meta-analysis. Being overweight was associated with an increased risk of COVID-19-related hospitalisations (OR 1.19, 95% CI 1.12 to 1.28, n=21 studies), but not death (OR 1.02, 95% CI 0.92 to 1.13, n=21). However, patients with obesity were at increased risk of both COVID-19-related hospitalisations (OR 1.72, 95% CI 1.62 to 1.84, n=58) and death (OR 1.25, 95% CI 1.19 to 1.32, n=77). Similarly, patients with extreme obesity were at increased risk of COVID-19-related hospitalisations (OR 2.53, 95% CI 1.67 to 3.84, n=12) and death (OR 2.06, 95% CI 1.76 to 3.00, n=19). There was a linear dose-response relationship between these obesity categories and COVID-19 outcomes, but the strength of the association has decreased over time.
Conclusion: Being overweight increases the risk of COVID-19-related hospitalisations but not death, while obesity and extreme obesity increase the risk of both COVID-19-related hospitalisations and death. These findings suggest that prompt access to COVID-19 care, prioritisation for COVID-19 vaccination and other preventive measures are warranted for this vulnerable group. © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  COVID-19

Year:  2022        PMID: 35814718      PMCID: PMC8783972          DOI: 10.1136/bmjnph-2021-000375

Source DB:  PubMed          Journal:  BMJ Nutr Prev Health        ISSN: 2516-5542


The study found a linear dose–response relationship between obesity categories and COVID-19 outcomes, in which the risk of COVID-19-related outcomes steadily increased with increasing levels of obesity. Studies with the most recent data showed a weaker association between obesity and COVID-19 outcomes compared with the earlier days of the pandemic. This decrease in the strength of the association follows the pattern of the first wave of COVID-19: Asian-Pacific, Europe and North America.

Introduction

Recently, a novel coronavirus named SARS-CoV-2, causing COVID-19, emerged in late 2019, and has posed a global threat with devastating consequences.1 2 To date, the disease is still spreading, new variants are emerging, breakthrough infections are being observed and the healthcare system is overwhelmed.2 As of 14 September 2021, there were 226 418 035 infected cases resulting in 4 657 736 deaths worldwide.3 The prognosis of COVID-19 has been consistently reported to worsen with older age, male sex and comorbidities such as diabetes, hypertension, chronic kidney disease, chronic respiratory disease and cardiovascular disease.4 These comorbidities are related to obesity and dysfunctional adipose tissue, thus predisposing people living with obesity to a greater risk of severe COVID-19. Studies have reported that adipose tissues are rich in ACE2 receptors, which act as a port of entry for SARS-CoV-2 to human cells.5 Additionally, obesity has been shown to alter immune function and increase the susceptibility to infection from different pathogens.6 More recently, several meta-analyses showed that obesity was associated with poor prognosis of COVID-19.7 8 However, these meta-analyses were limited by the number of included studies, ranging from 3 to 60, and mainly used body mass index (BMI) as a measure of obesity. Additionally, since the virus is changing, and the literature has been constantly evolving, it is important to reassess the risk of poor outcomes associated with obesity and summarise the current weight of evidence. This review aims to quantify the association between overweight or obesity and COVID-19-related hospitalisations (including hospital admission, intensive care unit (ICU) admission, invasive mechanical ventilation (IMV)) and death, and to assess the magnitude of the association and the potential dose–response relationships.

Methods

Protocol writing and registration

The protocol for this review was registered with the International Prospective Register of Systematic Reviews (identification number CRD42020198718). This systematic review was conducted based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement.9

Search strategy

We searched PubMed, Embase, Cochrane, Web of Sciences, WHO COVID-19 database, Google Scholar, followed by a hand search of the reference lists of related articles and reviews for studies published up to 20 July 2021. The search strategy included a combination of keywords and Medical Subject Headings (MeSH) for the concepts of COVID-19 and obesity. The following search strategy was used in PubMed and then adapted to other databases: (Covid-19 OR corona virus disease 2019 OR Novel corona virus OR novel corona OR SARS Cov-2 OR severe acute respiratory syndrome corona virus-2 OR 2019 novel coronavirus disease OR COVID-19 pandemic OR SARS-CoV-2 infection OR COVID-19 virus disease OR 2019 novel coronavirus infection OR 2019-nCoV infection OR coronavirus disease 2019 OR coronavirus disease-19 OR 2019-nCoV disease OR COVID-19 virus infection OR novel corona OR Wuhan coronavirus OR 2019 novel coronavirus OR 2019-nCoV OR Wuhan seafood market pneumonia virus OR COVID 19 virus OR coronavirus disease 2019 virus OR ‘SARS-CoV-2’[MeSH] OR ‘COVID-19’[MeSH]) AND (Obesity OR BMI OR Overweight OR over nutrition OR fat OR adiposity OR Body Mass index OR Weight OR height OR obese OR underweight OR normal weight OR malnutrition OR nutritional status OR Neck circumference OR Waist circumference OR Waist to hip ratio OR Visceral Adipose Tissue OR ‘obesity’[MeSH Terms] OR ‘overweight’[MeSH Terms] OR ‘nutritional status’[MeSH Terms] OR ‘adipose tissue’[MeSH Terms] OR ‘body mass index’[MeSH Terms] OR ‘malnutrition’[MeSH Terms] OR ‘waist circumference’[MeSH Terms] OR ‘intra-abdominal fat’[MeSH Terms] OR ‘waist-hip ratio’[MeSH Term]). Initial study eligibility was assessed by reviewing titles and abstracts and was carried out independently by two of the authors (WS/MT). These two authors then independently carried out full-text screening, with any disagreement being resolved by consulting a third author (TA).

Inclusion/exclusion criteria

The inclusion criteria included (1) cohort studies (prospective and retrospective), case–control studies and cross-sectional studies, (2) studies with effect estimates on the association between overweight or obesity and COVID-19 outcomes, (3) written in English, (4) peer reviewed, and (5) adjusted for at least one covariate. The exclusion criteria were (1) studies conducted in non-human subjects or in vitro, (2) infection of unspecific coronaviruses or other respiratory viruses, (3) duplicate studies or overlapping data, (4) articles without available full text or abstract only, and (5) commentaries and reviews.

Data extraction

We developed a standardised form to extract information from each study. The main components were the study characteristics (title, author, country, journal, publication date), the study design (design, sample size, participants, outcomes and exposure definition, covariates), the results (effect estimates and 95% CI) and limitations. Corresponding authors whose articles lack the above details were contacted via email for further information. Data were extracted by two authors (WS/MT) and verified by a third author (AG). Where multiple studies used the same data source, we included the study with the most recent data.

Exposure variable

BMI and non-BMI measures were used as indicators to reflect obesity status. Non-BMI-defined obesity included neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue. BMI-defined obesity included BMI as a continuous variable and categorised BMI. The categorisation was based on the geographic location of the included studies. For studies conducted in Asian-Pacific countries,10 normal weight was defined as BMI (18.5–22.9 kg/m2), overweight BMI (23–24.9 kg/m2), obese BMI ≥25 kg/m2 and extreme obese BMI ≥30 kg/m2. Similarly, for studies conducted in non-Asian-Pacific countries,11 normal weight was defined as BMI (18.5–24.9 kg/m2), overweight BMI (25–29.9 kg/m2), obese BMI ≥30 kg/m2 and extreme obese BMI ≥40 kg/m2.

Outcome variables

Diagnosis with SARS-CoV-2 was defined by a positive reverse transcription polymerase chain reaction (RT-PCR) assay from a nasopharyngeal sample. Three categories of outcomes were considered in the present analysis. The first category included studies that reported a single outcome such as hospital admission, ICU admission, intubation or IMV and death. The second category included studies that reported endpoints with two or more combinations of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease. In the third category, hospital admission, ICU and IMV were pooled to provide an estimate for COVID-19-related hospitalisations.

Covariates

Based on the current knowledge of the risk factors of severe COVID-19, we identified the following covariates as most important confounders: age, sex, race/ethnicity, socioeconomic status and comorbidities (cardiovascular diseases, diabetes mellitus, chronic kidney disease, chronic pulmonary diseases).

Quality assessment

The Newcastle-Ottawa Quality Assessment Scale was used to assess the risk of bias in the included studies. One reviewer (WS) independently assessed the quality of the studies, and a second reviewer (MT) verified the evaluation. Any disagreements were resolved by consulting a third reviewer (TA).

Data analysis

We summarised the associations between obesity and COVID-19-related outcomes through a random-effects meta-analysis using the methods suggested by DerSimonian and Laird.12 RevMan V.5.4 (Cochrane Collaboration) was used to analyse the data and associated adjusted ORs and 95% CIs were reported. Funnel plots were used to visually assess publication bias. Studies from the general population were analysed separately from studies of restricted (by age, sex, race/ethnicity, disease or condition) populations. The analysis was performed for obesity categories (overweight, obese, extreme obese) compared with normal weight or non-obese, and the outcomes of hospital admission, ICU, IMV, death and combinations of outcomes. We further combined obese versus normal weight and obese versus non-obese into obese and similarly for extreme obese. Then, we visually assess dose–response relationships by plotting the pooled OR versus obesity categories. An analysis by year of publication and geographic location was also performed. In a sensitivity analysis, we further restricted the data to cohort studies (prospective and retrospective) and prospective cohort studies.

Results

Description of included studies

After a full-text assessment, 208 studies were included in this meta-analysis (figure 1). The characteristics of the included studies are presented in table 1 and online supplemental table 1. A total of 3 550 977 participants from over 32 countries were included in this study. Seventy-seven studies were conducted in the USA, 19 in France, 17 in China, 14 in Italy, 14 in England, 11 in Mexico, 7 in Brazil and 6 in Spain. Ten studies were cross-sectional, 5 case–control and 193 cohort. Forty studies were conducted in a restricted population and 168 in the general population.
Figure 1

Flow chart of the literature selection process.

Table 1

Characteristics of included studies

CharacteristicsStudies (n)%
Country
 USA7737.02
 France199.13
 China178.17
 Italy146.73
 England146.73
 Mexico115.29
 Multi-county83.85
 Brazil73.37
 Spain62.88
 Netherlands41.92
 Korea31.44
 Germany, Ireland, Kuwait, Saudi Arabia, Turkey20.96
 Argentina, Australia, Chile, Colombia, Democratic Republic of Congo, Egypt, Iran, Israel, Japan, Libya, Morocco, Peru, Qatar, Scotland, Singapore, Switzerland, Thailand10.48
Study design
 Prospective cohort3516.83
 Retrospective cohort15875.96
 Case–control52.4
 Cross-sectional104.8
Study participants
 General population16880.77
 Restricted population*4019.23
Publication
 Studies published in 202012962.02
 Studies published in 20217937.98

*Restricted by age, sex, race/ethnicity, disease or condition.

Flow chart of the literature selection process. Characteristics of included studies *Restricted by age, sex, race/ethnicity, disease or condition.

Association between obesity categories and COVID-19 outcomes

Our results indicate that overweight was associated with higher odds of hospital admission (OR 1.22, 95% CI 1.07 to 1.39, n=7 studies), ICU (OR 1.20, 95% CI 1.01 to 1.43, n=12) and IMV (OR 1.22, 95% CI 1.09 to 1.37, n=12), giving a significant pooled OR for COVID-19-related hospitalisations (OR 1.19, 95% CI 1.12 to 1.28, n=21) (table 2 and online supplemental figure 1). However, there was no association between overweight and COVID-19 death (OR 1.02, 95% CI 0.92 to 1.13, n=21). Likewise, in the restricted population analysis (table 3), overweight was not associated with COVID-19-related hospitalisations (OR 1.03, 95% CI 0.90 to 1.17, n=5) and death (OR 1.01, 95% CI 0.88 to 1.16, n=5).
Table 2

Pooled estimate of the association between obesity and COVID-19 outcomes in the general population (n=168)

ExposureStudies with single outcomesStudies with combinations of outcomes*Hospital admission+ICU+IMV†
Hospital admissionICUIMVDeath
BMI continuous (5 units)
 Studies (n)25115135
 Pooled OR (95% CI)1.22 (1.16 to 1.28)1.28 (1.00 to 1.61)1.34 (1.16 to 1.54)1.10 (1.05 to 1.16)1.34 (1.16 to 1.61)1.28 (1.00 to 1.47)
Overweight versus normal weight
 Studies (n)7101221821
 Pooled OR (95% CI)1.22 (1.07 to 1.39)1.20 (1.01 to 1.43)1.22 (1.09 to 1.37)1.02 (0.92 to 1.13)1.18 (1.00 to 1.39)1.19 (1.12 to 1.28)
Obese versus normal weight
 Studies (n)8111127922
 Pooled OR (95% CI)1.40 (1.20 to 1.62)2.08 (1.51 to 2.87)2.15 (1.68 to 2.76)1.23 (1.11 to 1.37)1.44 (1.26 to 1.64)1.73 (1.53 to 1.97)
Obese versus non-obese
 Studies (n)122213501236
 Pooled OR (95% CI)1.67 (1.51 to 1.85)1.81 (1.55 to 2.12)1.65 (1.39 to 1.97)1.26 (1.19 to 1.34)1.93 (1.49 to 2.49)1.72 (1.60 to 1.85)
Extreme obese versus normal weight
 Studies (n)4421228
 Pooled OR (95% CI)1.98 (1.76 to 2.23)1.81 (1.08 to 3.05)3.03 (1.92 to 4.77)1.94 (1.63 to 2.20)1.69 (1.42 to 2.01)2.08 (1.53 to 2.81)
Extreme obese versus non-obese
 Studies (n)222724
 Pooled OR (95% CI)3.08 (1.60 to 5.92)3.95 (1.08 to 14.46)2.39 (1.96 to 2.91)2.37 (1.75 to 3.21)1.69 (1.31 to 2.19)3.19 (2.17 to 4.70)
Non-BMI-defined obesity‡
 Studies (n)032154
 Pooled OR (95% CI)1.79 (1.00 to 3.21)1.27 (1.13 to 1.42)2.00 (1.32 to 3.02)1.58 (1.14 to 2.20)1.32 (1.16 to 1.49)

*Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease.

†Pooled studies included in hospital admission, ICU and IMV.

‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue.

BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation.

Table 3

Pooled estimate of the association between obesity and COVID-19 outcomes in restricted (by age, sex, race/ethnicity, disease or condition) populations (n=40)

ExposureHospital admission+ICU+IMV*DeathStudies with combinations of outcomes†
BMI continuous (5 units)
 Studies (n)462
 Pooled OR (95% CI)1.16 (1.05 to 1.28)1.16 (1.05 to 1.34)1.69 (0.70 to 4.16)
Overweight versus normal weight
 Studies (n)553
 Pooled OR (95% CI)1.03 (0.90 to 1.17)1.01 (0.88 to 1.16)1.51 (0.89 to 2.58)
Obese versus normal weight
 Studies (n)552
 Pooled OR (95% CI)1.16 (0.92 to 1.45)1.03 (0.78 to 1.37)1.33 (0.99 to 1.80)
Obese versus non-obese
 Studies (n)698
 Pooled OR (95% CI)1.84 (1.43 to 2.37)1.88 (1.61 to 2.19)1.67 (1.29 to 2.15)
Extreme obese versus normal weight
 Studies (n)221
 Pooled OR (95% CI)1.33 (0.98 to 1.79)1.40 (1.13 to 1.72)1.22 (0.67 to 2.21)
Extreme obese versus non-obese
 Studies (n)001
 Pooled OR (95% CI)4.10 (1.28 to 13.11)
Non-BMI-defined obesity‡
 Studies (n)011
 Pooled OR (95% CI)10.71 (1.57 to 73.06)1.25 (0.98 to 1.59)

*Pooled studies included in-hospital admission, ICU and IMV. The estimates for hospital admission, ICU and IMV were not shown separately because of low number of studies.

†Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease.

‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue.

BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation.

Pooled estimate of the association between obesity and COVID-19 outcomes in the general population (n=168) *Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease. †Pooled studies included in hospital admission, ICU and IMV. ‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue. BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation. Pooled estimate of the association between obesity and COVID-19 outcomes in restricted (by age, sex, race/ethnicity, disease or condition) populations (n=40) *Pooled studies included in-hospital admission, ICU and IMV. The estimates for hospital admission, ICU and IMV were not shown separately because of low number of studies. †Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease. ‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue. BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation. Patients with obesity were at a high risk of COVID-19-related hospitalisations (OR 1.73, 95% CI 1.53 to 1.97, n=22) and death (OR 1.23, 95% CI 1.11 to 1.37, n=27) compared with normal weight (table 2 and online supplemental figure 1). Similar trends were observed comparing obese with non-obese, extreme obese with normal weight, extreme obese with non-obese and in non-BMI-defined obesity. Overall, the association between obesity categories and COVID-19 outcomes was stronger for COVID-19-related hospitalisations than death. In addition, the association was stronger in the general population than restricted population.

Dose–response association

We found that every 5-unit increase in BMI was associated with 28% increased odds of COVID-19-related hospitalisations (OR 1.28, 95% CI 1.00 to 1.47, n=5) and 10% increased odds of death (OR 1.10, 95% CI 1.05 to 1.16, n=15) suggesting a linear dose–response association (table 2 and online supplemental figure 1). The dose–response analysis confirmed that obesity categories were associated with COVID-19 outcomes in a linear dose–response manner (figure 2). The risk of poor COVID-19 outcomes steadily increased with increasing levels of obesity.
Figure 2

Dose-response association between obesity categories and COVID-19 outcomes. A) Hospital admission, B) ICU, C) IMV, D) Death, E) combinations of outcomes, F) Hospital admission + ICU + IMV. ICU, intensive care unit; IMV, invasive mechanical ventilation or intubation. Combinations of outcomes regroups studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disaese. Hospital admission + ICU + IMV is the pooled estimate of studies included in hospital admision, ICU and IMV.

Dose-response association between obesity categories and COVID-19 outcomes. A) Hospital admission, B) ICU, C) IMV, D) Death, E) combinations of outcomes, F) Hospital admission + ICU + IMV. ICU, intensive care unit; IMV, invasive mechanical ventilation or intubation. Combinations of outcomes regroups studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disaese. Hospital admission + ICU + IMV is the pooled estimate of studies included in hospital admision, ICU and IMV.

Low strength of the association over time

Studies with the most recent data showed a weaker association between obesity categories and COVID-19 outcomes compared with the earlier days of the pandemic. For example, comparing patients with obesity to normal weight, the adjusted OR for death was 1.31 (95% CI 1.10 to 1.57, n=17) in studies published in 2020 and 1.17 (95% CI 1.03 to 1.32, n=10) in studies published in 2021 (table 4). Furthermore, the strength of the association decreased following the pattern of the first wave of COVID-19 spread. For example, the association between obesity and COVID-19 death was 1.73 (95% CI 1.36 to 2.20, n=5) in Asian-Pacific countries, 1.43 (95% CI 1.14 to 1.79, n=24) in European countries and 1.13 (95% CI 1.04 to 1.22, n=31) in North American countries (table 5).
Table 4

Pooled estimate of the association between obesity and COVID-19 outcomes in the general population by publication year (n=168)

Exposure by publication yearHospital admission+ICU+IMV*DeathStudies with combinations of outcomes†
Studies (n)Pooled OR (95% CI)Studies (n)Pooled OR (95% CI)Studies (n)Pooled OR (95% CI)
BMI continuous (5 units)
 Studies published in 202021.34 (1.22 to 1.47)91.10 (1.05 to 1.16)71.47 (1.16 to 1.93)
 Studies published in 202131.28 (1.00 to 1.61)61.05 (0.86 to 1.28)61.34 (1.05 to 1.69)
Overweight versus normal weight
 Studies published in 2020111.30 (1.18 to 1.44)120.98 (0.90 to 1.06)11.60 (0.88 to 2.90)
 Studies published in 2021101.13 (1.05 to 1.21)91.18 (0.93 to 1.48)71.15 (0.97 to 1.37)
Obese versus normal weight
 Studies published in 2020131.76 (1.54 to 2.01)171.31 (1.10 to 1.57)21.58 (0.91 to 2.75)
 Studies published in 202191.57 (1.31 to 1.88)101.17 (1.03 to 1.32)71.45 (1.25 to 1.70)
Obese versus non-obese
 Studies published in 2020251.82 (1.58 to 2.10)331.29 (1.18 to 1.42)81.97 (1.33 to 2.92)
 Studies published in 2021121.65 (1.51 to 1.80)171.24 (1.16 to 1.33)41.94 (1.38 to 2.73)
Extreme obese versus normal weight
 Studies published in 202022.51 (1.85 to 3.42)61.98 (1.63 to 2.41)11.80 (1.47 to 2.20)
 Studies published in 202161.98 (1.43 to 2.73)61.89 (1.39 to 2.56)11.49 (1.11 to 2.00)
Extreme obese versus non-obese
 Studies published in 202032.30 (1.96 to 2.69)42.17 (1.49 to 3.17)21.69 (1.31 to 2.19)
 Studies published in 202115.55 (3.20 to 9.62)33.26 (1.61 to 6.62)0
Non-BMI-defined obesity‡
 Studies published in 202041.32 (1.16 to 1.49)031.80 (0.91 to 3.56)
 Studies published in 2021012.00 (1.32 to 3.02)21.50 (1.10 to 2.03)

*Pooled studies included in-hospital admission, ICU and IMV. The estimates for hospital admission, ICU and IMV were not shown separately because of low number of studies.

†Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease.

‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue.

BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation.

Table 5

Pooled estimate of the association between obesity and COVID-19 outcomes in the general population by region (n=150)

Exposure by regionHospital admission+ICU+IMV*DeathStudies with combinations of outcomes†
Studies (n)Pooled OR (95% CI)Studies (n)Pooled OR (95% CI)Studies (n)Pooled OR (95% CI)
BMI continuous (5 units)
 Asian-Pacific014.32 (1.05 to 17.9)52.49 (1.76 to 3.44)
 Europe31.28 (1.00 to 1.61)51.16 (1.00 to 1.28)31.22 (0.95 to 1.54)
 North America11.28 (1.16 to 1.47)81.05 (0.95 to 1.16)21.10 (0.90 to 1.28)
Overweight
 Asian-Pacific10.84 (0.46 to 1.55)10.53 (0.14, 2.00)31.16 (1.00 to 1.33)
 Europe32.11 (1.28 to 3.46)61.14 (0.93 to 1.39)21.68 (0.78 to 3.65)
 North America151.18 (1.10 to 1.25)141.00 (0.88 to 1.14)31.03 (0.82 to 1.29)
Obese
 Asian-Pacific32.35 (1.17 to 1.56)51.73 (1.36 to 2.20)92.37 (1.60 to 3.53)
 Europe142.64 (1.81 to 3.86)241.43 (1.14 to 1.79)51.42 (1.24 to 1.63)
 North America341.52 (1.45 to 1.59)411.13 (1.04 to 1.22)61.38 (1.18 to 1.62)
Extreme obese
 Asian-Pacific014.32 (1.37 to 13.61)0
 Europe24.08 (2.13 to 7.82)52.56 (2.11 to 3.11)12.30 (1.20 to 4.40)
 North America92.25 (1.91 to 2.65)131.81 (1.57 to 2.08)31.66 (1.44 to 1.93)
Non-BMI-defined obesity‡
 Asian-Pacific0012.47 (1.02 to 5.98)
 Europe41.32 (1.16 to 1.49)031.63 (1.00 to 2.66)
 North America012.00 (1.32 to 3.02)11.28 (0.92 to 1.79)

*Pooled studies included in-hospital admission, ICU and IMV. The estimates for hospital admission, ICU and IMV were not shown separately because of low number of studies.

†Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease.

‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue.

BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation.

Pooled estimate of the association between obesity and COVID-19 outcomes in the general population by publication year (n=168) *Pooled studies included in-hospital admission, ICU and IMV. The estimates for hospital admission, ICU and IMV were not shown separately because of low number of studies. †Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease. ‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue. BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation. Pooled estimate of the association between obesity and COVID-19 outcomes in the general population by region (n=150) *Pooled studies included in-hospital admission, ICU and IMV. The estimates for hospital admission, ICU and IMV were not shown separately because of low number of studies. †Studies whose endpoint was the combination of two or more of the following: hospital admission, ICU, IMV, death or other conditions pertaining to a severe disease. ‡Non-BMI-defined obesity includes neck circumference, waist circumference, waist-to-hip ratio and visceral adipose tissue. BMI, body mass index; ICU, intensive care unit; IMV, invasive mechanical ventilation.

Sensitivity analysis

The analysis from the general population further restricted to cohort studies (online supplemental table 2) and prospective cohort studies (online supplemental table 3) were consistent with the main analysis. In both analyses, being overweight was associated with an increased risk of COVID-19-related hospitalisations (OR 1.19, 95% CI 1.12 to 1.28, n=20 and OR 1.30, 95% CI 1.08 to 1.57, n=1), but not death (OR 1.00, 95% CI 0.90 to 1.10, n=20 and OR 1.09, 95% CI 0.94 to 1.26, n=6, respectively). Obesity and extreme obesity remained associated with COVID-19-related hospitalisations and death.

Assessment of quality and publication bias

All included studies had a quality score from the Newcastle-Ottawa Quality Assessment Scale ≥6, as shown in online supplemental table 1, which is acceptable for a meta-analysis. No outstanding bias was found from a visual inspection of the funnel plots (online supplemental figure 2).

Discussion

We found that being overweight increases the risk of COVID-19-related hospitalisations but not death while obesity and extreme obesity increase the risk of both COVID-19-related hospitalisations and death. In addition, there was a linear dose–response association between obesity categories and COVID-19 outcomes. However, the strength of the association has weakened over time following the pattern of the first wave of COVID-19. We included studies that used BMI as a continuous variable. To the best of our knowledge, this is the first meta-analysis to summarise studies that reported a continuous BMI. We found that the pooled estimate was consistent with the findings from the categorised BMI and the dose–response analysis. This finding of dose–response relationships should inform future causation studies. In the analysis restricted to the general population, we reached statistical significance for overweight and hospital admission, ICU and IMV, but not death. Yang et al found similar results concerning hospital admission (OR 2.09, 95% CI 1.22 to 3.60), IMV (OR 1.40, 95% CI 1.13 to 1.73) and death (OR 1.10, 95% CI 0.84 to 1.45), but did not reach statistical significance for ICU admission (OR 3.10, 95% CI 0.76 to 12.61).7 Another study by Yang et al 13 found a significant result for hospital admission (OR 1.30, 95% CI 1.09 to 1.57) with only two studies and reported results for death (OR 1.06, 95% CI 0.79 to 1.42) similar to our findings. In the restricted population, overweight was not associated with COVID-19-related outcomes. This null finding is probably due to the heterogeneity of this group. We found a significant association between obesity and extreme obesity with hospital admission, ICU, IMV and death. These results are consistent with the previous meta-analysis.7 8 However, we noticed a reduction in the strength of the association in general compared with previous studies.7 8 13 This might be due to our inclusion criteria which included only peer-reviewed studies that adjusted for at least one confounder. The relation between obesity and COVID-19 outcomes is confounded by variables such as age, sex and comorbidities, and adjusting for these variables could reduce the effect estimate. Additionally, studies with the most recent data showed a weaker association between obesity and COVID-19 outcomes compared with the earlier days of the pandemic. As the disease progressed, there has been an improvement in the care including better healthcare facilities preparedness, knowledge, and experience on clinical management, the finding of new drugs and increased public awareness about the disease transmission and prevention. Our finding of the association between non-BMI-defined obesity and COVID-19 outcomes adds to the literature. Systematic reviews including non-BMI obesity are rare with the highest number of included studies being 4.14 BMI, which is widely used to assess obesity, is often criticised as not reflecting an accurate adiposity status. Therefore, including studies that used non-BMI-defined obesity strengthens our results. The underlying mechanism by which obesity could increase the risk of severe COVID-19 has been discussed in numerous publications.5 6 15 First, adipose tissue could be a reservoir for viral production. This is because obesity is known to increase ACE2 expression which facilitates the cellular entry of SARS-CoV-2. Second, obesity is linked to impaired immune function which weakens the body that fails to contain viral replication. Third, obesity increases inflammation, which may have effects on the lung parenchyma and bronchi. Fourth, obesity decreases lung capacity and reserve and can make ventilation more difficult. This study is the largest and most comprehensive summary of the association between obesity and COVID-19 outcomes to date. We included BMI-defined and non-BMI-defined obesity and performed a dose–response, a geographic and publication period analysis. However, this study was not without limitations. First, the number of eligible studies under the extremely obese category and non-BMI-defined obesity was limited which has impacted the precision of the pooled estimate resulting in large CIs. Second, in the effort to reduce overlapping data, we excluded six large studies, but we could not rule out the possibility of residual participants’ overlap. Third, obesity status was dichotomised in some studies which could result in extreme obese participants being included in the obese group. Fourth, heterogeneity was high in the evaluated outcomes as expected. In addition, non-BMI-defined obesity studies were based on different scales and combining them might yield residual bias. Finally, most included studies were retrospective cohort and a causal relationship between obesity and COVID-19 outcomes would require further investigations.

Conclusion

This systematic review and meta-analysis revealed that overweight, obesity and extreme obesity increase the risk of poor COVID-19 outcomes in a dose–response manner. However, the magnitude of the association has weakened over time following the pattern of COVID-19 spread. Nevertheless, excess adiposity remains a significant risk factor of poor COVID-19 outcomes and required more attention. These findings suggest the importance of increased vigilance towards people with excess adiposity. Prompt access to COVID-19 testing and healthcare, prioritisation for COVID-19 vaccination and other preventive measures are warranted for this vulnerable group.
  14 in total

1.  Meta-analysis in clinical trials.

Authors:  R DerSimonian; N Laird
Journal:  Control Clin Trials       Date:  1986-09

2.  Covid-19: Delta infections threaten herd immunity vaccine strategy.

Authors:  Owen Dyer
Journal:  BMJ       Date:  2021-08-02

3.  Obesity and COVID-19: The Two Sides of the Coin.

Authors:  Dror Dicker; Silvia Bettini; Nathalie Farpour-Lambert; Gema Frühbeck; Rachel Golan; Gijs Goossens; Jason Halford; Grace O'Malley; Dana Mullerova; Ximena Ramos Salas; Maria N Hassapiou; Jørn Sagen; Euan Woodward; Volkan Yumuk; Luca Busetto
Journal:  Obes Facts       Date:  2020-07-13       Impact factor: 3.942

4.  Obesity Is a Risk Factor for Severe COVID-19 Infection: Multiple Potential Mechanisms.

Authors:  Naveed Sattar; Iain B McInnes; John J V McMurray
Journal:  Circulation       Date:  2020-04-22       Impact factor: 29.690

Review 5.  Factors Associated with Mortality in COVID-19 Patients: A Systematic Review and Meta-Analysis.

Authors:  Mojtaba Sepandi; Maryam Taghdir; Yousef Alimohamadi; Sima Afrashteh; Hadiseh Hosamirudsari
Journal:  Iran J Public Health       Date:  2020-07       Impact factor: 1.429

6.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.

Authors:  David Moher; Alessandro Liberati; Jennifer Tetzlaff; Douglas G Altman
Journal:  PLoS Med       Date:  2009-07-21       Impact factor: 11.069

7.  High Prevalence of Obesity in Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Requiring Invasive Mechanical Ventilation.

Authors:  Arthur Simonnet; Mikael Chetboun; Julien Poissy; Violeta Raverdy; Jerome Noulette; Alain Duhamel; Julien Labreuche; Daniel Mathieu; Francois Pattou; Merce Jourdain
Journal:  Obesity (Silver Spring)       Date:  2020-06-10       Impact factor: 9.298

8.  WHO Declares COVID-19 a Pandemic.

Authors:  Domenico Cucinotta; Maurizio Vanelli
Journal:  Acta Biomed       Date:  2020-03-19

9.  Visceral Adiposity Elevates the Risk of Critical Condition in COVID-19: A Systematic Review and Meta-Analysis.

Authors:  Mária Földi; Nelli Farkas; Szabolcs Kiss; Fanni Dembrovszky; Zsolt Szakács; Márta Balaskó; Bálint Erőss; Péter Hegyi; Andrea Szentesi
Journal:  Obesity (Silver Spring)       Date:  2021-02-02       Impact factor: 9.298

10.  Obesity aggravates COVID-19: An updated systematic review and meta-analysis.

Authors:  Jun Yang; Congmin Tian; Ying Chen; Chunyan Zhu; Hongyu Chi; Jiahao Li
Journal:  J Med Virol       Date:  2020-12-01       Impact factor: 20.693

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  4 in total

1.  Investigating the early impacts of the COVID-19 pandemic on modifiable risk factors for cancer and chronic disease: a repeated cross-sectional study in Alberta, Canada.

Authors:  Geneviève Jessiman-Perreault; Alvin Li; Nicole Frenette; Lisa Allen Scott
Journal:  Can J Public Health       Date:  2022-09-01

2.  Good practice statements for antithrombotic therapy in the management of COVID-19: Guidance from the SSC of the ISTH.

Authors:  Alex C Spyropoulos; Jean M Connors; James D Douketis; Mark Goldin; Beverley J Hunt; Taiwo R Kotila; Renato D Lopes; Sam Schulman
Journal:  J Thromb Haemost       Date:  2022-07-29       Impact factor: 16.036

3.  Association between obesity and COVID-19 mortality and length of stay in intensive care unit patients in Brazil: a retrospective cohort study.

Authors:  Vitor Barreto Paravidino; Tatiana Henriques Leite; Mauro Felippe Felix Mediano; Rosely Sichieri; Gulnar Azevedo E Silva; Victor Cravo; Alex Balduino; Emmanuel Salgueiro; Bruno Adler Maccagnan Pinheiro Besen; Rodrigo de Carvalho Moreira; Carlos Eduardo Brandão; Danilo Cosme Klein Gomes; Cinthia Almeida Guimarães Assemany; Pedro Cougo
Journal:  Sci Rep       Date:  2022-08-12       Impact factor: 4.996

4.  Body Mass Index and Risk for COVID-19-Related Hospitalization in Adults Aged 50 and Older in Europe.

Authors:  Maika Ohno; Dagmar Dzúrová
Journal:  Nutrients       Date:  2022-09-27       Impact factor: 6.706

  4 in total

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